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人类T淋巴细胞的分化。I. 在胸腺内正常T细胞成熟过程中获得一种新的人类细胞表面蛋白(p80)。

Differentiation of human T lymphocytes. I. Acquisition of a novel human cell surface protein (p80) during normal intrathymic T cell maturation.

作者信息

Haynes B F, Harden E A, Telen M J, Hemler M E, Strominger J L, Palker T J, Scearce R M, Eisenbarth G S

出版信息

J Immunol. 1983 Sep;131(3):1195-200.

PMID:6224850
Abstract

The thymus is thought to be the primary central lymphoid organ in which T cells mature. Although thymic cortical and medullary compartments are distinct histologically, few antigens have been described that are absolutely acquired during the presumed intrathymic maturation pathway from cortical to medullary thymocytes. In this paper, we describe the acquisition during human intrathymic T cell maturation of a novel protein (p80) defined by a monoclonal antibody (A1G3). Although the p80-A1G3 antigen is distributed throughout the body and is not T cell specific, our study demonstrates that expression of p80-A1G3 antigen in normal human thymus is associated with thymocyte functional maturity and location in the thymus medulla. Moreover, in contrast to other markers of mature human T cells, the p80-A1G3 cell surface protein is not expressed on T6+ cortical thymocytes, and, therefore, is absolutely acquired by medullary thymocytes during T cell maturation. Thus, the p80-A1G3 antigen and the A1G3 antibody provide a heretofore unavailable system for the study of molecular events that transpire during the maturation of thymocytes.

摘要

胸腺被认为是T细胞成熟的主要中枢淋巴器官。尽管胸腺皮质和髓质区域在组织学上是不同的,但很少有抗原被描述为在假定的从皮质胸腺细胞到髓质胸腺细胞的胸腺内成熟途径中绝对获得。在本文中,我们描述了一种由单克隆抗体(A1G3)定义的新型蛋白质(p80)在人胸腺内T细胞成熟过程中的获得情况。尽管p80 - A1G3抗原分布于全身且不是T细胞特异性的,但我们的研究表明,p80 - A1G3抗原在正常人胸腺中的表达与胸腺细胞功能成熟及在胸腺髓质中的位置相关。此外,与成熟人T细胞的其他标志物不同,p80 - A1G3细胞表面蛋白在T6 +皮质胸腺细胞上不表达,因此,在T细胞成熟过程中绝对是由髓质胸腺细胞获得的。因此,p80 - A1G3抗原和A1G3抗体为研究胸腺细胞成熟过程中发生的分子事件提供了一个前所未有的系统。

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